Deciphering the Electrocatalytic Activity of Nitrogen-Doped Carbon Embedded with Cobalt Nanoparticles and the Reaction Mechanism of Triiodide Reduction in Dye-Sensitized Solar Cells
- Authors
- Ahn, Sung Hee; Lee, Chi Ho; Kim, Min Soo; Kim, Seul Ah; Kang, Byungwuk; Kim, Hee-eun; Lee, Sang Uck; Bang, Jin Ho
- Issue Date
- Dec-2017
- Publisher
- American Chemical Society
- Citation
- Journal of Physical Chemistry C, v.121, no.49, pp 27332 - 27343
- Pages
- 12
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Journal of Physical Chemistry C
- Volume
- 121
- Number
- 49
- Start Page
- 27332
- End Page
- 27343
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/8385
- DOI
- 10.1021/acs.jpcc.7b09758
- ISSN
- 1932-7447
1932-7455
- Abstract
- The electrocatalytic activity of carbon materials for triiodide (I-3(-)) reduction has spurred the development of low-cost electrocatalysts as an alternative to platinum in dye-sensitized solar cells. While many catalytic aspects of nitrogen-doped carbons have been unveiled in recent years, not all underlying factors that dictate their electrocatalytic activity have been fully considered; the current understanding of the electrocatalytic activity of nitrogen-doped carbons is limited. In addition, the synergistic effect of metal nanoparticles embedded in nitrogen-doped carbon, which was recently demonstrated as a facile way to boost the electrocatalytic activity of carbon, remains elusive. This work sheds light on these unknown aspects of carbon's electrocatalytic activity by carrying out a systematic investigation of nitrogen-doped carbon with incorporated cobalt nanoparticles. Furthermore, the generally accepted mechanism of the I-3(-) reduction reaction (IRR) is re-evaluated in this work with the aid of density functional theory calculations and in-depth electrochemical analysis. A new insight into this mechanism, which suggests that there is another possible reaction pathway available for the IRR on carbon, is provided.
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